{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1362825893607766784.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/anie.199507131"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.199507131"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.199507131"}}],"dc:title":[{"@value":"Calixarenes, Macrocycles with (Almost) Unlimited Possibilities"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title><jats:p>The condensation reaction between<jats:italic>p‐tert</jats:italic>‐butylphenol and formaldehyde leads in a single step to good yields of cyclic oligomers in which, depending on the reaction conditions, either four, six, or eight phenol units are joined by methylene bridges. The beakerlike shape of the most stable conformation of the tetramer has led to their being given the name “calixarenes” (calix = chalice). Resorcinol can undergo condensation in a similar manner with a variety of aldehydes to afford cyclic tetramers with the same basic structure (the resorcarenes). In both cases the reaction does not require the use of dilution techniques, so that large quantities of product can be readily obtained. In addition, the parent compounds can be modified in various ways, in particular at the phenolic hydroxy groups or the phenyl residues; these approaches can be used separately or in combination. Calixarenes are thus ideal starting materials for the synthesis of various types of host molecules and can also act as building blocks for the construction of larger molecular systems with defined structures and functions. Their potential applications range from use as highly specific ligands for analytical chemistry, sensor techniques and medical diagnostics to their use in the decontamination of waste water and the construction of artificial enzymes and the synthesis of new materials for non‐linear optics or for ultrathin layers and sieve membranes with molecular pores.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1382825893607766784","@type":"Researcher","foaf:name":[{"@value":"Volker Böhmer"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"05700833"},{"@type":"PISSN","@value":"http://id.crossref.org/issn/14337851"}],"prism:publicationName":[{"@value":"Angewandte Chemie International Edition in English"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"1995-04-13","prism:volume":"34","prism:number":"7","prism:startingPage":"713","prism:endingPage":"745"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.199507131"},{"@id":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.199507131"}],"createdAt":"2004-01-16","modifiedAt":"2024-01-11","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050282677704065152","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A New Chiral Stationary Phase for Gas Chromatography by Use of a Chiral Thiacalix[4]arene Derivative"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219109163904","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis and Properties of Pentahomothiazacalix[3]arene Derivatives Constructed from Phenol-Formaldehyde Trimer and Aminoethanethiol Unit"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219109181440","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis and Binding Property of Tunable Upper-Rim Calix[4]crowns"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219109191936","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Exploitation of Na+-Selective Electrodes for Protein Solutions from Crown-Bridged Calix[4]quinones"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219109771904","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Design of Homooxacalix[3]arene–Porphyrin Heterocapsules Which Provide Novel Cavities for Molecular Recognition"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233577378432","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A rhomboid-shaped organic host molecule with small binding space. 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